Binding and relaxation behaviour of Prodan and Patman in phospholipid vesicles: A fluorescence and H-1 NMR study

被引:57
作者
Hutterer, R
Schneider, FW
Sprinz, H
Hof, M
机构
[1] CHARLES UNIV, INST PHYS CHEM, CZ-12840 PRAGUE 2, CZECH REPUBLIC
[2] UNIV WURZBURG, INST PHYS CHEM, D-97070 WURZBURG, GERMANY
[3] UNIV LEIPZIG, MAX PLANCK SOC, GRP TIME RESOLVED SPECT, D-04318 LEIPZIG, GERMANY
关键词
time-dependent Stokes shift; dielectric solvent relaxation; head group dynamics; high resolution H-1 NMR; Prodan; Patman;
D O I
10.1016/S0301-4622(96)02185-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relative location, binding behaviour and the solvent relaxation behaviour of the polarity sensitive membrane probes 6-propionyl-2-(dimethylamino)naphthalene and 6-palmitoyl-2-[[trimethylammoniumethyl]methylamino]naphthalene chloride in vesicles composed of 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine or egg yolk lecithin have been compared using steady-state and time-resolved fluorescence as well as high resolution NMR measurements. The reconstructed time-resolved emission spectra show unambiguously that the observed spectral shifts in vesicle systems have to be assigned to time-dependent solvent relaxation processes rather than to a probe relocation mechanism. All fluorescence as well as the NMR relaxation data suggest a deeper localization of Patman in the membrane, sensing a less polar and/or more restricted probe environment.
引用
收藏
页码:151 / 160
页数:10
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